EXPEDIUM 279763080Recalls & reported problems
Medos International Sàrl · EXPEDIUM SPINE SYSTEM DISTRACTOR, PARALLEL ACTION 6.35 · Class 1
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10705034200750), received between Apr 19, 2024 and Apr 19, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 19, 2024Break; Break
IT WAS REPORTED THAT ON UNKNOWN DATE THE INSTRUMENT WAS BROKEN. THERE WAS NO PATIENT OUTCOME REPORTED. THIS REPORT IS FOR ONE DISTRACTOR, PARALLEL ACTION. THIS IS REPORT 1 OF 5 FOR COMPLAINT (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19143763 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.